CRISPR/Cas12a and primer-assisted rolling circle amplification integrated ultra-sensitive dual-signal sensing platform for EGFR 19 detection

被引:12
作者
Deng, Liyuan [1 ]
Zhou, Shiying [1 ]
Dong, Jiangbo [1 ]
Liu, Yin [1 ]
Huang, Zhen [4 ,5 ]
Sun, Human [1 ]
Jin, Liang [1 ]
Huo, Danqun [1 ,2 ]
Hou, Changjun [1 ,3 ]
机构
[1] Chongqing Univ, Bioengn Coll, Key Lab Biorheol Sci & Technol, State & Local Joint Engn Lab Vasc Implants,Minist, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Sch Microelect & Commun Engn, Chongqing Key Lab Biopercept & Intelligent Informa, Chongqing 400044, Peoples R China
[3] Shanghai Jiao Tong Univ, Natl Facil Translat Med, Shanghai 200240, Peoples R China
[4] Sichuan Univ, SeNA Res Inst, Coll Life Sci, Key Lab Bioresource & Ecoenvironm,Minist Educ, Chengdu 610000, Peoples R China
[5] Szostak CDHT Large Nucl Acids Inst, Chengdu 610000, Peoples R China
关键词
EGFR; 19; Rolling circle amplification (RCA); CRISPR/Cas12a; Dual-signal sensor platform; METAL-ORGANIC FRAMEWORKS; ABUNDANCE;
D O I
10.1016/j.aca.2023.341755
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, we integrated CRISPR/Cas12a with primer-assisted rolling circle amplification (PARCA) to specifically detect EGFR 19 from the genome. We fused the method into fluorescent and electrochemical detection systems forming a stable and sensitive dual-signal sensing platform. The fluorescent detection system stably detected EGFR 19 in a linear range from 500 fM to 10 nM with an ultra-low background signal. The electrochemical detection system possessed a detection limit as low as 42 aM due to the introduction of nanomaterial UIO-66- NH2. The dual-signal sensing platform showed superior performance in complex serum samples and real cell genomes and provided a flexible and dynamic approach for the ultra-sensitive detection of EGFR 19.
引用
收藏
页数:8
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